HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → Ethyl 3-difluoromethyl-1-methyl-4-pyrazole carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | HCID 10103284 | HCID 10103284 | — |
| Reactant | Ethanamine, 1,1,2,2-tetrafluoro-N,N-dimethyl- | HCID 21945697 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 3-difluoromethyl-1-methyl-4-pyrazole carboxylate | HCID 11644126 | 80.9% |
Reaction Steps
10.8 g of N-1,1,2,2-tetrafluoroethyldimethylamine were initially charged in 50 ml of acetonitrile under argon and 26 g of boron trifluoride as a 17% solution in CH3CN were added at RT. The mixture was stirred for 30 min and then admixed with 8.67 g of ethyl dimethylaminoacrylate. The mixture was stirred at RT for 2 h and then added slowly to the solution of 3.4 g of methylhydrazine in 10 ml of acetonitrile at 10° C. After stirring at RT for 2 h, the acetonitrile was removed completely under reduced pressure and the product was admixed with water and filtered off. Distillation under reduced pressure or washing with cyclohexane afforded 10 g of the product with the purity of 99% and an m.p. of 62-63° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939673B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-59bffec6e2ec4b758a5caaa65d47ea30 |
| Source note | uspto-grants-2011_05 |